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IDEAYA Biosciences to Announce Topline Results from Phase 2/3 OptimUM-02 Trial in Metastatic Uveal Melanoma on Monday, April 13, 2026

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Rhea-AI Sentiment
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earnings date clinical trial

IDEAYA (NASDAQ: IDYA) will release topline results from the Phase 2/3 OptimUM-02 trial on Monday, April 13, 2026 at 8:00 a.m. ET. The trial evaluates darovasertib plus crizotinib in first-line HLA*A2-negative metastatic uveal melanoma.

A joint IDEAYA and Servier pre-market release will be followed by a conference call and webcast; a replay will be available on IDEAYA's website for 30 days.

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AI-generated analysis. Not financial advice.

Positive

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Negative

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News Market Reaction – IDYA

+7.61%
11 alerts
+7.61% News Effect
+16.0% Peak in 6 min
+$189M Valuation Impact
$2.68B Market Cap
0.0x Rel. Volume

On the day this news was published, IDYA gained 7.61%, reflecting a notable positive market reaction. Argus tracked a peak move of +16.0% during that session. Our momentum scanner triggered 11 alerts that day, indicating notable trading interest and price volatility. This price movement added approximately $189M to the company's valuation, bringing the market cap to $2.68B at that time.

Data tracked by StockTitan Argus on the day of publication.

Key Figures

Trial phase: Phase 2/3 Topline call time: 8:00 a.m. ET Webcast replay duration: 30 days
3 metrics
Trial phase Phase 2/3 OptimUM-02 registrational trial design
Topline call time 8:00 a.m. ET Scheduled conference call on April 13, 2026
Webcast replay duration 30 days Replay availability on IDEAYA’s website

Market Reality Check

Price: $28.21 Vol: Volume 1,416,043 vs 20-da...
normal vol
$28.21 Last Close
Volume Volume 1,416,043 vs 20-day average 1,031,341 (relative volume 1.37) ahead of the topline readout announcement. normal
Technical Shares at $31 are trading above the 200-day MA of $29.67, sitting 21.08% below the 52-week high and 130.48% above the 52-week low.

Peers on Argus

Sector peers show mixed moves (e.g., DNLI -0.41%, BLTE +2.57%, TVTX +1.19%), and...

Sector peers show mixed moves (e.g., DNLI -0.41%, BLTE +2.57%, TVTX +1.19%), and the momentum scanner reports no coordinated sector move, indicating this scheduled Phase 2/3 readout is primarily stock-specific.

Historical Context

5 past events · Latest: Apr 06 (Positive)
Pattern 5 events
Date Event Sentiment Move Catalyst
Apr 06 Phase 1 trial start Positive -1.2% First-patient-in for Phase 1 IDE574 KAT6/7 inhibitor solid tumor trial.
Mar 30 Combination trial start Positive +3.3% First-patient-in for IDE849 and IDE161 Phase 1 combination in DLL3 tumors.
Mar 27 Inducement option grants Neutral -5.1% Inducement stock options totaling 49,000 shares to new employees.
Mar 18 Conference presentations Positive -2.8% AACR 2026 poster abstracts for multiple Phase 1 programs announced.
Mar 09 Phase 1 trial start Positive +5.7% First-patient-in for IDE892 PRMT5 inhibitor and MTAP/CDKN2A updates.
Pattern Detected

Recent clinically focused updates often saw mixed to negative next-day price reactions, even when news described pipeline progress.

Recent Company History

Over the last month, IDEAYA issued multiple pipeline and corporate updates. Three Phase 1 “first-patient-in” clinical trial announcements on Mar 9, Mar 30, and Apr 6 produced varied 24-hour moves from -1.22% to +5.69%. News on stock option and inducement grants in late March saw negative reactions of -5.08% and -2.8%. Against this backdrop of active development across programs, today’s scheduled Phase 2/3 topline darovasertib readout represents a more advanced, potentially pivotal catalyst.

Market Pulse Summary

The stock moved +7.6% in the session following this news. A strong positive reaction aligns with the...
Analysis

The stock moved +7.6% in the session following this news. A strong positive reaction aligns with the significance of a Phase 2/3 registrational readout for darovasertib in metastatic uveal melanoma. The stock previously showed mixed responses to earlier-stage updates, with 24-hour moves from -5.08% to +5.69%, so a larger move around topline data could reflect the higher stakes. Investors would also weigh recent insider net buying of 50,000 shares and the company’s extensive late-stage pipeline.

Key Terms

phase 2/3, registrational trial, metastatic uveal melanoma, hla*a2-negative
4 terms
phase 2/3 medical
"their ongoing Phase 2/3 registrational trial, OptimUM-02, evaluating darovasertib"
A phase 2/3 trial is a combined clinical study that first evaluates how well a treatment works and the best dose, then expands into a larger test to confirm those results and safety. For investors, it matters because moving into a phase 2/3 signals that an experimental therapy has shown initial promise and will be tested at scale, which can materially change the odds and timeline for regulatory approval and commercial potential.
registrational trial medical
"ongoing Phase 2/3 registrational trial, OptimUM-02, evaluating darovasertib"
A registrational trial is the large, definitive clinical study designed to provide the evidence regulators need to decide whether a new drug or medical product can be approved for sale. Think of it as the final exam for a treatment: passing it can unlock widespread market access and potential revenues, while failing it can sharply reduce a product’s commercial prospects and raise investment risk.
metastatic uveal melanoma medical
"in patients with first-line HLA*A2-negative metastatic uveal melanoma."
Metastatic uveal melanoma is an eye cancer that begins in the uvea (the eye’s middle layer) and has spread to other parts of the body, most often the liver. For investors, it matters because the spread makes the disease much harder to treat, so clinical trial results, regulatory approvals, and new therapies can dramatically change a drug developer’s prospects—think of a small house fire that spreads to the whole neighborhood, changing the value of nearby properties.
hla*a2-negative medical
"in patients with first-line HLA*A2-negative metastatic uveal melanoma."
HLA-A2-negative means an individual does not carry the HLA-A2 version of a common immune-system gene. HLA types act like locks on cells that determine which immune-targeted therapies and vaccines can engage a patient’s immune system, so being HLA-A2-negative can make a person ineligible for treatments or clinical trials designed for HLA-A2 carriers, which affects the potential patient pool and commercial market for those therapies.

AI-generated analysis. Not financial advice.

SOUTH SAN FRANCISCO, Calif., April 10, 2026 /PRNewswire/ -- IDEAYA Biosciences, Inc. (NASDAQ: IDYA), a precision medicine oncology company, today announced plans to issue a joint IDEAYA and Servier pre-market press release and host a conference call and webcast on Monday, April 13, 2026 at 8:00 a.m. ET to disclose topline results from their ongoing Phase 2/3 registrational trial, OptimUM-02, evaluating darovasertib in combination with crizotinib in patients with first-line HLA*A2-negative metastatic uveal melanoma. The call will include members of IDEAYA's management joined by a distinguished key opinion leader.

Conference Call and Webcast Information

The webcast registration information can be accessed using this link or by visiting the Events section of the IDEAYA website. A replay of the webcast will be available on IDEAYA's website for 30 days following the live event.

About IDEAYA Biosciences

IDEAYA is a precision medicine oncology company committed to the discovery, development, and commercialization of transformative therapies for cancer. Our approach integrates expertise in small-molecule drug discovery, structural biology and bioinformatics with robust internal capabilities in identifying and validating translational biomarkers to develop tailored, potentially first-in-class targeted therapies aligned to the genetic drivers of disease. We have built a deep pipeline of product candidates focused on synthetic lethality and antibody-drug conjugates, or ADCs, for molecularly defined solid tumor indications. Our mission is to bring forth the next wave of precision oncology therapies that are more selective, more effective, and deeply personalized with the goal of altering the course of disease and improving clinical outcomes for patients with cancer. IDEAYA's corporate presentation is available on its website: https://ir.ideayabio.com/ 

Investor and Media Contact

IDEAYA Biosciences 
Joshua Bleharski, Ph.D.
Chief Financial Officer
investor@ideayabio.com

Cision View original content to download multimedia:https://www.prnewswire.com/news-releases/ideaya-biosciences-to-announce-topline-results-from-phase-23-optimum-02-trial-in-metastatic-uveal-melanoma-on-monday-april-13-2026-302739365.html

SOURCE IDEAYA Biosciences, Inc.

FAQ

When will IDEAYA (IDYA) announce OptimUM-02 topline results and how can I listen?

IDEAYA will announce topline results on April 13, 2026 at 8:00 a.m. ET. According to IDEAYA, a joint pre-market release with Servier will precede a live conference call and webcast, with a replay available on IDEAYA's website for 30 days.

What patient population does the OptimUM-02 trial reported by IDEAYA (IDYA) cover?

The OptimUM-02 trial enrolled first-line HLA*A2-negative patients with metastatic uveal melanoma. According to IDEAYA, the study tests darovasertib in combination with crizotinib in that specific patient population.

What treatments are being evaluated in IDEAYA's (IDYA) OptimUM-02 Phase 2/3 trial?

OptimUM-02 is evaluating darovasertib plus crizotinib in combination therapy. According to IDEAYA, the Phase 2/3 registrational trial studies this combination in first-line HLA*A2-negative metastatic uveal melanoma.

Will IDEAYA (IDYA) provide materials or a replay after the OptimUM-02 results call?

Yes. According to IDEAYA, the company and Servier will issue a pre-market press release and host a webcast; a replay will be available on IDEAYA's website for 30 days following the live event.

Who will present on IDEAYA's (IDYA) OptimUM-02 results call and webcast?

IDEAYA management will present and will be joined by a key opinion leader. According to IDEAYA, the call will include company executives and an external expert to discuss topline OptimUM-02 results.